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Trial record 26 of 31 for:    Bardoxolone methyl OR CDDO-Me OR RTA 402

A Double-Blind, Randomized, Placebo-Controlled Study Evaluating the Effects of Bardoxolone Methyl on Body Composition in Patients With Stage 4 Chronic Kidney Disease and Type 2 Diabetes Mellitus

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01655186
Recruitment Status : Withdrawn (IDMC recommendation for safety concerns)
First Posted : August 1, 2012
Last Update Posted : October 23, 2012
Information provided by (Responsible Party):
Reata Pharmaceuticals, Inc.

Brief Summary:
This multicenter, randomized, double-blind, placebo-controlled Phase 2 safety study will assess the effect of bardoxolone methyl relative to placebo on body weight and fat mass in approximately 60 patients with stage 4 Chronic Kidney Disease (CKD) and Type 2 Diabetes Mellitus (T2DM).

Condition or disease Intervention/treatment Phase
Renal Insufficiency, Chronic Diabetes Mellitus, Type 2 Drug: Bardoxolone Methyl Drug: Placebo Phase 2

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 0 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Study Start Date : September 2012
Actual Primary Completion Date : October 2012
Estimated Study Completion Date : October 2013

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Kidney Diseases

Arm Intervention/treatment
Placebo Comparator: Placebo
Oral, once daily
Drug: Placebo
Experimental: Bardoxolone Methyl
Oral, once daily
Drug: Bardoxolone Methyl

Primary Outcome Measures :
  1. Mean change in body weight as measured by Dual Energy X-ray Absorptiometry (DXA) [ Time Frame: Baseline, Weeks 12 and 24 ]
    DXA to be done 14 days prior to or after the weeks 12 and 24 visits

Secondary Outcome Measures :
  1. Mean change in fat mass as measured by Dual Energy X-ray Absorptiometry (DXA) [ Time Frame: Baseline, Weeks 12 and 24 ]
    DXA to be done 14 days prior to or after the weeks 12 and 24 visits

  2. Change in visceral fat mass measured by Magnetic Resonance Imaging of the abdomen [ Time Frame: Baseline and Week 24 ]
    MRI to be done 14 days prior to or after the week 24 visit

  3. Change in hepatic fat mass as measured by Magnetic Resonance Imaging of the liver [ Time Frame: Baseline and Week 24 ]
    MRI to be done 14 days prior to or after the week 24 visit

  4. Change in left ventricular structure and function as measured by gated Magnetic Resonance Imaging of the heart [ Time Frame: Baseline, Weeks 12 and 24 ]
    MRI to be done 14 days prior to or after the weeks 12 and 24 visits

  5. Change in gait speed [ Time Frame: Baseline, Weeks 12 and 24 ]
  6. Frequency, intensity and relationship of study drug to adverse events and serious adverse events, as well as clinical, and laboratory test result abnormalities [ Time Frame: 24 weeks ]

Information from the National Library of Medicine

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Ages Eligible for Study:   30 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  1. Screening eGFR ≥ 15.0 and < 30.0 mL/min/1.73 m2; screening eGFR will be the average of the eGFR values collected during screening;
  2. A history of type 2 diabetes mellitus; diagnosis must have been made at ≥ 30 years of age;
  3. Male or female patients at least 30 years of age;
  4. Treatment with an angiotensin converting enzyme (ACE) inhibitor and/or an angiotensin II receptor blocker (ARB) for at least 6 weeks prior to Screening Visit A and during screening. The dosage of ACE inhibitor and/or ARB must be at KDOQI goal dose (Appendix 13.4) and stable for 2 weeks prior to Screening Visit A and during screening (i.e., no change in dosage or medication);
  5. Mean systolic blood pressure (SBP) must be ≤ 160 mmHg and ≥ 105 mmHg and mean diastolic blood pressure (DBP) must be < 90 mmHg during screening visits A and B;
  6. Willing to practice methods of birth control (both males who have partners of childbearing potential and females of childbearing potential) during screening, while taking study drug and for at least 30 days after the last dose of study drug is ingested;
  7. Serum magnesium level must be greater than or equal to 1.3 mEq/L at Screening Visit B or during a subsequent unscheduled visit during screening (serum magnesium level may be re-evaluated once during an unscheduled visit);
  8. Willing and able to give written informed consent for study participation and cooperate with all aspects of the protocol including tolerating being in a closed MRI.

Exclusion Criteria:

Type 1 diabetes mellitus. If a history of diabetic ketoacidosis exists, a fasting C-peptide level must confirm type 2 diabetes; 2. Known non-diabetic renal disease (e.g., polycystic kidney disease, focal segmental glomerulosclerosis) [nephrosclerosis superimposed on diabetic kidney disease is acceptable]; Ongoing clinical investigation with evidence (e.g., unexplained hematuria or red blood cell or white blood cell casts) suggesting non-diabetic renal disease other than nephrosclerosis; 4. History of a renal transplant or a planned transplant from a living donor during the study; 5. Urine albumin/creatinine ratio (UACR) at Screening Visit B greater than 3500 mg/g; 6. Hemoglobin A1c level > 11.0% during screening; 7. Acute dialysis or acute kidney injury within 12 weeks prior to screening or during screening; 8. Clinical signs and/or symptoms of uremia and expected need for renal replacement therapy within 12 weeks following randomization, as assessed by the investigator; 9. Recently active cardiovascular disease defined as:

  • Unstable angina pectoris within 12 weeks before study randomization;
  • Myocardial infarction, coronary artery bypass graft surgery, or percutaneous transluminal coronary angioplasty/stent within 12 weeks before study randomization;
  • Cerebrovascular accident, including transient ischemic attack, within 12 weeks before study randomization;
  • Current diagnosis of Class III or IV NYHA congestive heart failure (Appendix 13.3); 10. Clinical diagnosis of severe obstructive valvular heart disease or severe obstructive hypertrophic cardiomyopathy; 11. Atrioventricular block, 20 or 30; 12. Implanted medical device that would prevent obtaining a MRI; 13. Administration of a contrast agent that may induce nephropathy within 30 days prior to study randomization or planned during the study; 14. Systemic immunosuppression for more than 2 weeks, cumulatively, within the 12 weeks prior to randomization or anticipated need for immunosuppression during the study; 15. Total bilirubin, aspartate transaminase (AST), or alanine transaminase (ALT) level greater than the upper limit of normal (ULN) or alkaline phosphatase level greater than two times the ULN on ANY screening laboratory test result; 16. Female patients who are pregnant, intend to become pregnant during the study, or are nursing; 17. BMI < 18.5 kg/m2; 18. Weight ≥ 300 pounds; 19. Height > 6'3"; 20. Partial or total amputation of a lower extremity prior to randomization; 21. Known hypersensitivity to any component of the study drug; 22. Current history of drug or alcohol abuse, as assessed by the investigator; 23. Clinically significant infection requiring intravenous administration of antibiotics or hospitalization within 6 weeks prior to Screening Visit A or during screening; 24. Hepatitis B surface antigen positive; Diagnosis or treatment of a malignancy in the past 5 years, excluding non-melanoma skin cancer and carcinoma in situ of the cervix or a condition highly likely to transform into a malignancy during the course of the study; 26. History of bariatric surgery or planned bariatric surgery during the course of the study; 27. A clinical condition that, in the judgment of the investigator, could potentially pose a health risk to the patient while involved in the study; 28. Participation in a clinical study involving any intervention within 30 days prior to randomization, concurrent participation in such a study, or participation in a prior clinical study involving bardoxolone methyl in any form; 29. Unable to communicate or cooperate with the investigator due to language problems, poor mental development, or impaired cerebral function.

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Responsible Party: Reata Pharmaceuticals, Inc. Identifier: NCT01655186     History of Changes
Other Study ID Numbers: 402-C-1202
First Posted: August 1, 2012    Key Record Dates
Last Update Posted: October 23, 2012
Last Verified: October 2012

Keywords provided by Reata Pharmaceuticals, Inc.:
Chronic Kidney Disease
Type 2 Diabetes Mellitus

Additional relevant MeSH terms:
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Diabetes Mellitus
Kidney Diseases
Diabetes Mellitus, Type 2
Renal Insufficiency, Chronic
Renal Insufficiency
Glucose Metabolism Disorders
Metabolic Diseases
Endocrine System Diseases
Urologic Diseases